Target intelligence / Profile preview

Patient-specific melanoma-associated antigens and tumor-associated antigens presented by autologous dendritic cells (DC-MAA/TAA vaccine)

Target
DC-MAA/TAA vaccine
Molecular classification
Antigen, MHC-peptide complex, Cellular therapy
01

Overview

Patient-specific melanoma-associated antigens and tumor-associated antigens presented by autologous dendritic cells refers to a personalized cellular immunotherapy platform rather than a single molecular target. This therapeutic strategy involves harvesting a patient's own dendritic cells (DCs) and loading them ex vivo with a cocktail of antigens, including shared tumor-associated antigens (TAAs) like MART-1 or gp100, and unique neoantigens identified through tumor sequencing (Sahin & Türeci, 2018; PubMed: 29298440). These pulsed dendritic cells are then matured and re-administered to the patient, where they migrate to lymph nodes and present the antigens to naive T cells via MHC Class I and II molecules (Banchereau & Steinman, 1998; PubMed: 9521314). This process primes a specific and robust cytotoxic T lymphocyte (CTL) response designed to recognize and eliminate melanoma cells throughout the body (NCI Drug Dictionary, 2023). The approach is designed to overcome tumor-induced immunosuppression by providing high-quality antigen presentation that the patient's endogenous system may lack (Nature Reviews Cancer, 2021; PubMed: 34168333). Clinical applications primarily focus on treating metastatic melanoma or preventing recurrence in high-risk patients (Journal of Clinical Oncology, 2019; PubMed: 31013171).

Other names
Personalized melanoma vaccineAutologous dendritic cell vaccineNeoantigen-pulsed dendritic cell vaccineDC-based melanoma immunotherapy
02

Mechanism of action

Autologous dendritic cells are loaded with patient-specific antigens and re-infused to present these antigens via MHC molecules to T cells, thereby inducing a targeted cytotoxic immune response against melanoma cells.

03

Biological functions

Immune responseAntigen presentationT-cell activationCytotoxic T lymphocyte priming
04

Disease associations

Melanoma
05

Safety considerations

Injection site reactionsFlu-like symptomsAutoimmune-related adverse events (e.g., vitiligo)Manufacturing complexity and failureLogistical challenges of autologous sourcing
06

Interacting drugs

TLPLDC (Tumor Lysate, Particle-Loaded, Dendritic Cell)

3 more in the full profile.

07

Biomarkers

Tumor Mutational Burden (TMB)HLA-A*02:01 statusInterferon-gamma (IFN-g) productionT-cell receptor (TCR) sequencing

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